Find research datasets worth reusing
Search datasets from major research repositories and use ShareScore to quickly assess how well each record supports discovery, access, and reuse.
1,432
datasets available to search
ShareScore release 0.9.0
Dataset results
1,432 results for “data type”
MCR LTER: Coral Reef: Material legacy disturbance type model; data for Kopecky et al., 2023 Ecology
This data package contains the code necessary to create a mathematical model of coral reef recovery dynamics following different types and intensities of disturbances that either remove dead coral skeletons (e.g., tropical storms) or leave standing dead skeletons (e.g., coral bleaching) and run associated analyses. We explored the sensitivity of the model to variation in key parameters, such as the strength of herbivory, and the degree to which dead skeletons protect algae from herbivory. Further, we assessed disturbance intensities and values of these parameters that lead to shifts between coral and macroalgae-dominated reefs. This code was published in Ecology and were a part of the thesis of K. Kopecky (2023). Analyses and full methods descriptions of this model can be found in the manuscript “Material legacies can degrade resilience: Structure-retaining disturbances promote regime shifts on coral reefs” (DOI: https://doi.org/10.1002/ecy.4006). No novel data were used or generated in this study. This manuscript uses data collected by the U.S. National Science Foundation's (NSF) Moorea Coral Reef Long Term Ecological Research (MCR LTER) site under Grant No. OCE 2224354 (and earlier awards). Additional financial support to the MCR LTER site was provided through a generous gift from the Gordon and Betty Moore Foundation. Research was completed under permits issued by the French Polynesian Government (Délégation à la Recherche) and the Haut-commissariat de la République en Polynésie Francaise (DTRT) (Protocole d'Accueil 2005-2023).
Deep splicing plasticity of the human adenovirus type 5 transcriptome as a driver of virus evolution nanopore data 48hpi
<p>Adenovirus infected MRC5 cells direct RNA sequencing of the mRNA using nanopore. From the paper Deep splicing plasticity of the human adenovirus type 5 transcriptome as a driver of virus evolution. Both the uncorrected fastq files and the lordec corrected files together with the normalised illumina data used to correct the nanpore data are here.</p>
Data set for Global quantitative synthesis of ecosystem functioning across climatic zones and ecosystem types
<p>Dataset used in the publication: " Global quantitative synthesis of ecosystem functioning across climatic zones and ecosystem types". The dataset gathers estimates of ecosystem standing stocks (biomass, organic carbon, detritus), fluxes (GPP, ER, NEP) and process rates (decomposition and carbon uptake rates) for eight broad ecosystem types (forest, grassland, agroecosystem, desert, stream, lake, pelagic and benthic marine ecosystems) in five broad climatic zones (arctic, boreal, arid, temperate, tropical, arid).</p> <p>The scripts to produce the figures and the statistics of the publication are released along with the txt version of the data, which file is uploaded when running the script.</p>
Supplementary data to accompany Information flow, cell types and stereotypy in a full olfactory connectome
<p>Supplemental file 1</p> <p>Layers assigned by the probabilistic graph traversal model. bodyId refers to neurons’ unique ID in ne- uPrint. layer mean contains the mean layer after 10,000 iterations of the main model (Figure 2). layer - olf mean and layer th mean contain the mean layers from running the traversal model with ORNs and THN/HRNs, respectively (Figure S2).</p> <p>S1 hemibrain neuron layers.csv</p> <p>Supplemental file 2</p> <p>Sensory meta-information related to each glomerulus. Columns: glomerulus (canonical name for one of the 51 olfactory + 7 thermo/hygrosensory antennal lobe glomeruli), laterality (whether the glomerulus receives bilateral or only unilateral innervation from ALRNs), expected cit (a citation that describes the expected number of RNs in this glomerulus), expected RN female 1h (number of expected RNs in one hemi- sphere), expected RN female SD (standard deviation in the expected number of RNs), missing (qualitative assessment of glomeruli truncation), RN frag (if the RNs in that glomerulus are fragmented), receptor (the OR or IR expressed by cognate ALRNs (Bates et al., 2020; Task et al., 2020)), odour scenes (the general ‘odour scene(s)’ which this glomerulus may help signal (Mansourian and Stensmyr, 2015; Bates et al., 2020)), key ligand(the ligand that excites the cognate ALLRN or receptor the most, based on pooled data from multiple studies (Mu ̈nch and Galizia, 2016)), valence (the presumed valence of this odour chan- nel (Badel et al., 2016)). Exists as hemibrain glomeruli summary in our R package hemibrainr.</p> <p>S2 hemibrain olfactory information.csv</p> <p>Supplemental file 3</p> <p>File listing all identified antennal lobe receptor neurons (ALRNs) in the hemibrain, including information shown in neuPrint. See above for column explanations. Exists as rn.info in our R package hemibrainr.</p> <p>S3 hemibrain ALRN meta.csv</p> <p>Supplemental file 4</p> <p>All the hemibrain neurons we have classed as antennal lobe local neurons (ALLNs). See above for column explanations. Exists as alln.info in our R package hemibrainr.</p> <p>S4 hemibrain ALLN meta.csv</p> <p>Supplemental file 5</p> <p>All the hemibrain neurons we have classed as antennal lobe projection neurons (ALPNs). See above for column explanations. In addition, across dataset cluster refers to the clustering with left and right FAFB PNs; is canonical indicates whether that ALPN is one of the well studied “canonical” uPNs. Exists as pn.info in our R package hemibrainr.</p> <p>40</p> <p>S5 hemibrain ALPN meta.csv</p> <p>Supplemental file 6</p> <p>All the hemibrain neurons we have classed as third-order olfactory neurons (TOONs) including lateral horn neurons (LHNs), as well as wedge projection neurons (WEDPNs), lateral horn centrifugal neurons (LHCENT) and other projection neuron classes (Figure 1). See above for column explanations. Exists as ton.info in our R package hemibrainr.</p> <p>S6 hemibrain TOON meta.csv</p> <p>Supplemental file 7</p> <p>All the hemibrain neurons we have classed as neurons that descend to the ventral nervous system (DNs). See above for column explanations. Exists as dn.info in our R package hemibrainr.</p> <p>S8 hemibrain DN meta.csv</p> <p>Supplemental file 8</p> <p>The root point in hemibrain voxel space, for each hemibrain neuron. This is either the location of the soma, or the tip of a severed cell body fibre tract, where possible. Exists as hemibrain somas in our R package hemibrainr.</p> <p>S8 hemibrain root points.csv</p> <p>Supplemental file 9</p> <p>The start points for different neuron compartments. Nodes downstream of this position in the 3D structure of the neuron indicated with bodyid, belong to the compartment type designated by Label. A product of running flow centrality on hemibrain neurons, exists as hemibrain splitpoints in our R package hemi- brainr.</p> <p>S9 hemibrain compartment startpoints.csv</p> <p>Supplemental file 10</p> <p>3D triangle mesh for the hemibrain surface as a .obj file. This mesh was generated by first merging individual ROI meshes from neuPrint and then filling the gaps in between in a semi-manual process. It also exists as hemibrain.surf in our R package hemibrainr.</p> <p>S10 hemibrain raw.obj</p> <p>Supplemental file 11</p> <p>3D meshes of 51 olfactory + 7 thermo/hygrosensory antennal lobe glomeruli for the hemibrain volume, generated from ALRN presynapses.</p> <p>41</p> <p>Note that hemibrain coordinate system has the anterior-posterior axis aligned with the Y axis (rather than the Z axis, which is more commonly observed).</p> <p>S11 hemibrain AL glomeruli meshes RN-based.zip</p> <p>Supplemental file 12</p> <p>3D meshes of 51 olfactory + 7 thermo/hygrosensory antennal lobe glomeruli for the hemibrain volume, generated from ALPN presynapses.</p> <p>Note that hemibrain coordinate system has the anterior-posterior axis aligned with the Y axis (rather than the Z axis, which is more commonly observed).</p> <p>These meshes are also available as hemibrain al.surf in our R package hemibrainr. S12 hemibrain AL glomeruli meshes PN-based.zip</p>
Data for Cell-type-specific inhibitory circuitry from a connectomic census of mouse visual cortex
<p>Data for the paper: Cell-type-specific inhibitory circuitry from a connectomic census of mouse visual cortex, Nature 640, 2025</p> <p>In brief, this data archive includes information about the skeleton morphology and synaptic features of neurons whose cell bodies fell within a 100 micron by 100 micron column spanning all layers of mouse visual cortex. See <a href="https://www.microns-explorer.org/cortical-mm3">MICrONs-Explorer</a> for a full description of the broader volume and how it was collected.</p> <p>The data here include both data tables of cell locations, neuronal features, synapse lists, and more, as well as files containing morphological descriptions of all neurons used for the analysis in the initial version of the preprint. See the README.md file for more complete information about the individual files.</p> <p>Note: Data has been updated with post-publication files.</p>
A fading radius valley towards M-dwarfs, a persistent density valley across stellar types -- data
Open the record for dataset details and reuse information.
Replication data for: "The hapax / type ratio: an indicator of minimally required sample size in productivity studies?"
<p>The dataset accompanies the scientific article "The hapax / type ratio: an indicator of minimally required sample size in productivity studies?" and can be used to reproduce the findings presented in this article. This dataset consists of two components, namely (i) the corpus data involving the Dutch semi-copular verb "raken" and (ii) an R analysis script to reproduce the computational steps.</p>
Data from calculated radial neutron flux distributions in a KBS-3 type geological repository
<p>Data from calculations of radial distribution of neutron flux per emitted neutron from rods of spent nuclear fuel in a KBS-3 type geological repository. Reference (<em>Jansson, 2022</em>) contain a summary of the calculations and a description of the structure of this data.</p> <p>This data was computed on resources provided by Swedish National Infrastructure for Computing (SNIC) at Uppsala Multidisciplinary Center for Advanced Computational Science (UPPMAX), National Supercomputer Centre at Linköping University (NSC) and the SNIC Cloud, partially funded by the Swedish Research Council through grant agreement no. 2018-05973, under projects SNIC 2021/5-299 and SNIC 2021/18-12.</p>
Supporting data for: Type 1 diabetes risk genes mediate pancreatic beta cell survival in response to proinflammatory cytokines
<p><strong>SUMMARY OF THE STUDY</strong></p> <p>We combined functional genomics and human genetics to investigate processes that affect type 1 diabetes (T1D) risk by mediating beta-cell survival in response to proinflammatory cytokines. We mapped 38,931 cytokine-responsive candidate <em>cis-</em>regulatory elements (cCREs) in beta-cells using ATAC-seq and snATAC-seq and linked them to target genes using co-accessibility and HiChIP. Using a genome-wide CRISPR screen in EndoC-βH1 cells we identified 867 genes affecting cytokine-induced survival, and genes promoting survival and up-regulated in cytokines were enriched at T1D risk loci. Using SNP-SELEX, we identified 2,229 variants in cytokine-responsive cCREs altering transcription factor (TF) binding, and variants altering binding of TFs regulating stress, inflammation and apoptosis were enriched for T1D risk. At the 16p13 locus, a fine-mapped T1D variant altering TF binding in a cytokine-induced cCRE interacted with <em>SOCS1</em>, which promoted survival in cytokine exposure. Our findings reveal processes and genes acting in beta-cells during inflammation that modulate T1D risk.</p> <p><strong>DESCRIPTION OF FILES:</strong></p> <ul> <li>Supplementary Data 1. List of islet cCREs annotated with cell type and cytokine response - also in GSE205853</li> <li>Supplementary Data 2. Coaccessible sites in untreated beta cells and promoter annotations - also in GSE205853</li> <li>Supplementary Data 3. Coaccessible sites in cytokine-treated beta cells and promoter annotations - also in GSE205853</li> <li>Supplementary Data 4. Coaccessible sites in cytokine treated and untreated beta cells and promoter annotations - also in GSE205853</li> <li>Supplementary Data 5. Chromatin interactions in EndoC-BH1 cells - also in GSE205853</li> <li>Supplementary Data 6. Variants selected for SNP-SELEX assay </li> <li>Supplementary Data 7. Variants with TF binding and allelic binding results from SNP-SELEX</li> <li>Supplementary Data 8. snATAC-seq barcodes and metadata - also in GSE205853</li> <li>Supplementary Data 9. CRISPR-KO screen results - also in GSE205853</li> <li>Supplementary Data 10. Bulk ATAC-seq count matrix - also in GSE205853</li> <li>Supplementary Data 11. Bulk RNA-seq count matrix - also in GSE205853</li> <li>Supplementary Data 12. Alpha cells snATAC-seq count matrix - also in GSE205853</li> <li>Supplementary Data 13. Acinar cells snATAC-seq count matrix - also in GSE205853</li> <li>Supplementary Data 14. Beta cells snATAC-seq count matrix - also in GSE205853</li> <li>Supplementary Data 15. Stellate cells snATAC-seq count matrix - also in GSE205853</li> <li>Supplementary Data 16. Endothelial cells snATAC-seq count matrix - also in GSE205853</li> <li>Supplementary Data 17. Delta cells snATAC-seq count matrix - also in GSE205853</li> <li>Supplementary Data 18. Luciferase assay rs10483809</li> <li>Supplementary Data 19. SOCS1 knockdown qPCR results</li> <li>Supplementary Data 20. SOCS1 knockdown Apotracker (flow-cytometry)results</li> </ul> <p><strong>Raw data deposited at GEO, accessions GSE205853 and GSE118725.</strong></p> <p><em>Please refer to publication and GEO for details on methods.</em></p>
Data from: Will Current Protected Areas Harbour Refugia for Threatened Arctic Vegetation Types until 2050? A First Assessment
<p>We present predictions of Arctic vegetation for 2050 based on a combination of climate models (namely, EC-Earth3-Veg, IPSL-CM6A-LR, and MRI-ESM2-0), emission scenarios (names, SSP126 and SSP585) and tree dispersal rate scenarios (unrestricted, 20km and 5km) based on the methods of Pearson et al. (2013) and the new raster version of the Circumpolar Arctic Vegetation Map (CAVM) (Raynolds et al. 2019). We additionally present a dataset summarising total areas for each vegetation type in the CAVM and the forecasted models based on the computation of zonal histograms in ArcGIS (zonal_histogram_results.csv), for the total Arctic as well as only within protected areas, defined by the Map of Arctic Protected Areas (CAFF and PAME 2017). We also present a potential map of refugia for what we deem the realistic model (IPSL, SSP585, 20 km tree dispersal) as a raster file. Refugia were identified as regions where the vegetation remained the same between the CAVM and the predictions. Additionally, we present a map of model agreement, showing the degree to which other models agree with the vegetation classification for our refugia.</p> <p>All predictions named according to the tree dispersal rate, climate model, and emissions scenario, preceded by the term "pred". For example: "pred_unres_mri_585" represents the unrestricted tree dispersal, MRI-ESM-0 climate model, and SSP585 scenario-based prediction. The MRI-ESM-0 x SSP585 combination had gaps in data which results in a lack of predictions in some areas; this affects 3 models.</p> <p>Further details and all code associated with these datasets are found <a href="https://github.com/PlekhanovaElena/Arctic_vegetation_prediction">here</a>.</p>
Rare type III responses: data & data methods (v1.0.0)
<p>This repository includes the data (data-rare-type3-responses.csv) for Kalinkat et al. (2023).</p> <p>The data comprises a literature review on type III functional responses between 2002 and 2022 with 12 variables and 107 observations. Please read the accompanying document (Rall_et_al_2023_Zenodo_Rare-type3-responses_data_methods_v1_0_0.pdf) for the methods and a description of the variables. </p> <p><strong>Reference</strong></p> <p>Kalinkat, G. <em>et al.</em> (2023) ‘Empirical evidence of type III functional responses and why it remains rare’, <em>Frontiers in Ecology and Evolution</em>, 11:1033818. Available at: https://doi.org/10.3389/fevo.2023.1033818.</p>
Raw data to "Series expansions in closed and open quantum many-body systems with multiple quasiparticle types"
<p>This collection of data is complementary to the publication "Series expansions in closed and open quantum many-body systems with multiple quasiparticle types", Lea Lenke, Andreas Schellenberger, Kai Phillip Schmidt, <a href="https://arxiv.org/abs/2302.01000">arXiv:2302.01000</a> (<a href="https://arxiv.org/abs/2302.01000">https://arxiv.org/abs/2302.01000</a>).</p> <p>It contains all data used for Figure 2 given in the file `Figure_2_complementary_data.yaml` and all needed data to recalculate the energies of the visualized modes in the files `Figure_2_coefficients_expectation_values.yaml` and `Figure_2_broad_signum_coefficients_expectation_values.yaml`.</p> <p>For the last two files, we used a program to calculate the coefficients. The source code for coefficient calculation is openly available under GitHub (<a href="https://github.com/FAU-kpslab/pcstpp_CoefficientGenerator">https://github.com/FAU-kpslab/pcstpp_CoefficientGenerator</a>) including configuration files to reproduce the coefficients given here.</p> <p>All files are self-consistent, for further information we recommend the comments directly in the files.</p> <p>For further details on the used method pcst<sup>++ </sup>and discussion of the results we refer to the linked publication.</p> <p>If any question may arise, you are highly welcome to contact us (see e.g. contact information on the publication).</p>
Data on different types of green spaces and their accessibility in the seven largest urban regions in Finland
<p>This repository contains data described in the article "Data on different types of green spaces and their accessibility in the seven largest urban regions in Finland" (Heikinheimo et al. 2023) and used in the research article "Associations of neighborhood-level socioeconomic status, accessibility, and quality of green spaces in Finnish urban regions" (Viinikka et al. 2023). <br> <br> This repository contains data on green space quality and path distances to different types of green spaces. The path distances represent green space accessibility using active travel modes (walking, cycling). The path distances were calculated using the pedestrian street network across the seven largest urban regions in Finland. We derived the green space typology from the Urban Atlas Data that is available across functional urban areas in Europe and enhanced it with national data on water bodies, conservation areas and recreational facilities and routes from Finland. We extracted the walkable street network from OpenStreetMap and calculated shortest paths to different types of green spaces using open-source Python programming tools. Network distances were calculated up to ten kilometers from each green space edge and the distances were aggregated into a 250 m x 250 m statistical grid that is interoperable with various statistical data from Finland. The geospatial data files representing the different types of green spaces, network distances across the seven urban regions, as well as the processing and analysis scripts are shared in an open repository. These data offer actionable information about green space accessibility in Finnish city regions and support the integration of green space quality and active travel modes into further research and planning activities.</p> <p> </p> <p><strong>Data description article: </strong></p> <p>Heikinheimo, V., Tiitu, M., & Viinikka, A. (2023). Data on different types of green spaces and their accessibility in the seven largest urban regions in Finland. <em>Data in Brief</em>, <em>50</em>, 109458. <a href="https://doi.org/10.1016/j.dib.2023.109458">https://doi.org/10.1016/j.dib.2023.109458</a></p> <p><strong>Related research article:</strong> </p> <p>Viinikka, A., Tiitu, M., Heikinheimo, V., Halonen, J. I., Nyberg, E., & Vierikko, K. (2023). Associations of neighborhood-level socioeconomic status, accessibility, and quality of green spaces in Finnish urban regions. <em>Applied Geography</em>, <em>157</em>, 102973. <a href="https://doi.org/10.1016/j.apgeog.2023.102973">https://doi.org/10.1016/j.apgeog.2023.102973</a></p>
Seedling emergence and biomass data of nine dryland plant species characterizing the impact of soil residual auxin herbicide across two soil types and water pulse events on greenhouse growth; Las Cruces, New Mexico, Spring 2021.
Synthetic-auxin herbicides are often used to control woody plants and aid in grassland restoration. Seed-based restoration is common alongside herbicide applications and there may be unintended effects of these herbicides on dryland plant species at the seed and seedling stages. Additionally, abiotic conditions at the time of herbicide application may influence herbicide-soil-plant interactions. We conducted a greenhouse study to examine the effects of a common shrub-control herbicide mix and its interaction with soil type and a post-herbicide water pulse on common desert plant seeds and seedlings. In this greenhouse study, we found that a subset of species responded negatively to soil residual herbicide activity of a mixture of aminopyralid, clopyralid, and triclopyr at the seed and seedling stages. Species sensitive to soil herbicide residues were primarily shrub and forb species that are often the target species of herbicide applications for woody plant control, such as Prosopis glandulosa (honey mesquite) and Larrea tridentata (creosote bush). However, two shrub species (Atriplex canescens [four-wing saltbush] and Yucca elata [soaptree yucca]) and one perennial grass species (Digitaria californica [Arizona cottontop]), which are used in dryland restoration projects, were found to be particularly sensitive to soil residual herbicide activity. Thus, if using these herbicides to control woody plants and restore herbaceous vegetation via active seeding or relying on the in situ seed bank, considerations should be given to what species are used in the seed mix, what species are already present in the soil seed bank, and other details of the circumstances of herbicide application.
Data: Algorithms for new types of fair stable matchings
<p>This data corresponds to the data and experiments described in Section 5 of<br> the following paper:</p> <p>Algorithms for new types of fair stable matchings<br> Authors: Frances Cooper and David Manlove</p> <ul> <li>The paper is located at: <a href="https://arxiv.org/abs/2001.10875">https://arxiv.org/abs/2001.10875</a></li> <li>The software is located at: <a href="https://zenodo.org/record/3630383">https://zenodo.org/record/3630383</a></li> <li>The data is located at: <a href="https://zenodo.org/record/3630349">https://zenodo.org/record/3630349</a></li> </ul> <p>See the README for more information.</p>
Data supplement for "Bifurcations of front motion in passive and active Allen-Cahn-type equations"
<p>This dataset contains the data and source files for figures 5 and 7-10 in the following publication: </p> <p>F. Stegemerten, S.V. Gurevich, U. Thiele</p> <p><em>'Bifurcations of front motion in passive and active Allen–Cahn-type equations' </em></p> <p>published in 2020 in CHAOS.</p> <p>Please follow the instructions given in 'Readme.txt'.</p>
Data set for "Cell-type-specific nicotinic input disinhibits mouse barrel cortex during active sensing"
<p>Data set for: Gasselin C, Hohl B, Vernet A, Crochet C, Petersen CCH (2021) Cell-type-specific nicotinic input disinhibits mouse barrel cortex during active sensing. Neuron doi: 10.1016/j.neuron.2020.12.018</p> <p>There are 2 files in this upload:</p> <p>1. The file named "2021_Gasselin_Neuron.pdf" is the Open Access pdf of the online publication in Neuron.</p> <p>2. The file named "Gasselin_data_code.zip" (~9 GB) is a zipped version of a folder "Gasselin_data_code" (~13 GB), which contains the data analysed in the study along with the Matlab code used to generate the published figures. To access the data and the code, first unzip the file. Then add the folder with subfolders to the Matlab path and run the different codes. The current folder must be the main folder (‘Gasselin_data_code’). Each code computes and plots the results used in the corresponding figure. Figures and Tables are saved in the subfolder ‘Figures’.</p> <p>The subfolder ‘Functions’ contains functions called by the main codes.</p> <p>The main folder contains the following codes:</p> <p><em>Gasselin_Figure1: computes and plots the results for the panels D, E and F of figure 1.</em></p> <p><em>Gasselin_Figure2: computes and plots the results for the panels B and C of figure 2.</em></p> <p><em>Gasselin_Figure3: computes and plots the results for the panels B, C and D of figure 3.</em></p> <p><em>Gasselin_Figure4: computes and plots the results for the panels A, B and C of figure 4.</em></p> <p><em>Gasselin_FigureS1: computes and plots the results for the panels A, B and C of figure S1.</em></p> <p><em>Gasselin_FigureS2: computes and plots the results for the panels A and B of figure S2.</em></p> <p> </p> <p>The subfolder ‘Data’ contains the data structures used for the different figures:</p> <p><em>data_figure1.mat</em></p> <p><em>data_figure2.mat</em></p> <p><em>data_figure3.mat</em></p> <p><em>data_figure4_MECA.mat</em></p> <p><em>data_figure4_Activation.mat</em></p> <p><em>data_figure4_Inactivation.mat</em></p> <p><em>data_figureS2_Activation.mat</em></p> <p><em>data_figureS2_Inactivation.mat</em></p> <p><em>data_Axon.mat</em></p> <p> </p> <p>The data structures contain the following fields:</p> <p><em>Mouse_Name</em> : name of the mouse.</p> <p><em>Mouse_DateOfBirth</em>: date of birth of the mouse (YMD).</p> <p><em>Mouse_Sex</em>: sex of the mouse (F or M).</p> <p><em>Mouse_Genotype</em>: genotype of the mouse.</p> <p><em>Mouse_Drug</em>: experimental condition of the recording (control = ‘No Drug’; blockade of glutamatergic transmission = ‘CNQX_DAPV’; blockade of glutamatergic transmission and nicotinic receptors = ‘CNQX_DAPV_MECA’; blockade of nicotinic receptors only = ‘MECA’).</p> <p><em>Mouse_Virus</em>: virus injected if any.</p> <p><em>Cell_Counter</em>; cell recorded in a given mouse.</p> <p><em>Cell_Type</em>: type of the recorded cell based on 2P imaging. (EXC, VIP, PV, SST, 5HT3aR_non_VIP).</p> <p><em>Cell_Depth</em>: depth of the recorded cell relative to pia (µm).</p> <p><em>Cell_TargetedBrainArea</em>: cortical area targeted (C2 column of the barrel cortex = C2).</p> <p><em>Cell_Fluorescence</em>: expression of the genetically encoded fluorophore (FALSE or TRUE). A neuron recorded in a VIP_IRES_Cre x LSL_tdTomato (cf <em>Mouse_Genotype</em>) with <em>Cell_Fluorescence</em>=TRUE is considered as a VIP neuron (cf <em>Cell_Type</em>).</p> <p><em>Sweep_Counter</em>: number of the sweep recorded for a given neuron (data were acquired across successive continuous sweeps of 30-60 s).</p> <p><em>Sweep_Type</em>: experimental condition during that sweep (Only spontaneous whisking onset = ‘Onset’; Whisking onset and whisker stimulus = ‘Onset_Whisker_Stim’ ; Optogenetic stimulation = ‘Opto_Stim’; Optogenetic activation = ‘Opto_Activation’; Optogenetic inactivation = ‘Opto_Inactivation’; ).</p> <p><em>Sweep_Start_Time</em>: time at the beginning of the sweep recording (YMDHms).</p> <p><em>Sweep_WhiskerAngle</em>: C2 whisker angular position extracted from simultaneous high-speed video filming (deg).</p> <p><em>Sweep_WhiskerAngle_SamplingRate</em>: sampling rate of the whisker angle trace.</p> <p><em>Sweep_WhiskingOnset_Time</em>: time of identified whisking onset - excluding any whisker stimulus shortly before or after (s).</p> <p><em>Sweep_MembranePotential</em>: membrane potential recording (mV) after cutting of the APs.</p> <p><em>Sweep_MembranePotential_SamplingRate</em>: sampling rate of the membrane potential signal (pt.s<sup>-1</sup>).</p> <p><em>Sweep_CurrentInjected</em>: current injected into the cell (pA).</p> <p><em>Sweep_CurrentInjected_SamplingRate</em>: sampling rate of current signal (pt.s<sup>-1</sup>).</p> <p><em>Sweep_WhiskerStim_Name</em>: whisker to which the magnetic stimulus was applied to (C2 or B2&C2).</p> <p><em>Sweep_WhiskerStim_Time</em>: onset times of the whisker stimulus (s).</p> <p><em>Sweep_OptoStim_Power</em>: light power applied for optogenetic manipulations (% of the max power).</p> <p><em>Sweep_OptoStim_Time</em>: onset times of the light pulses for optogenetic manipulations (s).</p> <p><em>Cell_ID</em>: unique cell identifier (= <em>Mouse_Name</em>+<em>Cell_Counter</em>).</p> <p><em>SpikeThreshold</em>: spike threshold used to detect APs (mV).</p> <p><em>Trial_WhiskingOnset</em>: data structure containing the cut signals used to compute averaged responses around whisking onset times.</p> <p><em>Trial_WhiskerStim</em>: data structure containing the cut signals used to compute averaged responses around whisker stimulus onset times.</p> <p><em>Trial_WhiskerStim_QuietTrials</em>: data structure containing the cut signals used to compute averaged responses around whisker stimulus onset times for trials without whisker movements.</p> <p><em>Trial_WhiskerStim_WhiskingTrials</em>: data structure containing the cut signals used to compute averaged responses around whisker stimulus onset times for trials with whisker movements.</p> <p><em>Trial_Opto</em>: data structure containing the cut signals used to compute averaged responses around optogenetic stimulus onset times.</p> <p><em>Trial_OptoAndWhisker_QuietTrials</em>: data structure containing the cut signals used to compute averaged responses around whisker stimulus onset times for trials with optogenetic manipulation and no whisker movements.</p> <p><em>Trial_OptoAndWhisker_WhiskingTrials</em>: data structure containing the cut signals used to compute averaged responses around whisker stimulus onset times for trials with optogenetic manipulation and with whisker movements.</p> <p><em>Trial_OnlyWhisker_QuietTrials</em>: data structure containing the cut signals used to compute averaged responses around whisker stimulus onset times for trials without optogenetic manipulation and without whisker movements.</p> <p><em>Trial_OnlyWhisker_WhiskingTrials</em>: data structure containing the cut signals used to compute averaged responses around whisker stimulus onset times for trials without optogenetic manipulation and with whisker movements.</p> <p><em>Trial_OnlyOpto</em>: data structure containing the cut signals used to compute averaged responses around optogenetic stimulus onset times in trials without whisker stimulus.</p>
Data licences and organization type of contributors to the Global Biodiversity Information Facility as of 19 January 2016
<p>Data from the Global Biodiversity Information Facility were extracted using R (version 3.2.0) on 9 July 2015 using the rgbif package (version 0.9.0) (Chamberlain, S., Ram, K., Barve, V. & Mcglinn, D. (2015) Package ‘rgbif’: Interface to the Global 'Biodiversity' Information Facility 'API' http://cran.r-project.org/web/packages/rgbif/rgbif.pdf). The ‘rights’ statements was extracted for all occurrence datasets with one or more observations. A total of 12,458 datasets were extracted, but only about 11% of the datasets have an explicit data-useage-rights statement at the dataset level. However, some datasets use the occurrence level ‘rights’ and ‘accessRights’ fields. To extract these data the rights information was obtained from the first record of each dataset where a rights statement was missing at the dataset level.</p> <p>The datasets were categorized into 13 different types depending on the origin of the observations.</p> <ol> <li>Biodiversity Information Facility or data centre</li> <li>Botanical Garden or Herbarium</li> <li>Citizen science</li> <li>Commercial</li> <li>Data publisher</li> <li>Educational</li> <li>Government</li> <li>Museum</li> <li>Network</li> <li>Parks Authority or Nature Reserve</li> <li>Research institution</li> <li>Society</li> <li>Foundations</li> </ol>
The data behind the ApJ article "Environmental Dependence of Type Ia Supernovae in Low-Redshift Galaxy Clusters"
<p>Data from "Environmental Dependence of Type Ia Supernovae in Low-Redshift Galaxy Clusters", <a href="https://ui.adsabs.harvard.edu/abs/2023arXiv230601088L/abstract">NASA ADS</a></p><p>inner_cluster_data.csv and outer_cluster_data.csv include the SALT3 mB, x1, and c parameter values, distance moduli and Hubble residuals (with _1 referring to Figure 9 and _2 referring to Figure 10), outlier designation from MCMC procedure, host cluster, host cluster redshift (with Hubble diagram version converted to frame of CMB), host cluster r500, projected separation from cluster center, NED Host galaxy name, photometrically-derived estimate for host mass, host or SN redshift used in analysis, and the Host SFR category (Q: quiescent, SF: star-forming, GV: green valley) for our cluster SNe Ia.</p><p>sf_field.csv and quiescent_field.csv contain SALT parameter values, distance moduli and Hubble residuals (from Figure 10), host galaxy sSFR and mass measurements, and host redshifts (all spectroscopic, also with Hubble diagram converted values) for SNe Ia in our field samples.</p><p>full_cluster.csv contains the data from the table in the appendix of the paper.</p><p>The inner_cluster_/outer_cluster_mcmc_samples.csv files contain the samples needed to reproduce the corner plot for Figure 10.</p><p>The Python scripts recreate the figures from the paper given the above data. The details for which columns and constraints needed to reproduce the figures are included in these files.</p>
Fetal exposure to the Ukraine famine of 1932-1933 and adult Type 2 Diabetes Mellitus (Public data and analytical code)
<p><strong>Abstract</strong></p> <p>The short-term impact of famines on death and disease is well documented but it is difficult to estimate their potential long-term impact. We used the setting of the man-made Ukrainian Holodomor famine of 1932-1933 to examine the relationship between prenatal famine and adult Type 2 diabetes mellitus (T2DM). This ecological study included 128,225 T2DM cases diagnosed between 2000-2008 among 10,186,016 male and female Ukrainians born between 1930 and 1938. Individuals who were born in the first half-year of 1934, and hence exposed in early gestation to the mid-1933 peak famine period, had a larger than two-fold likelihood of T2DM (OR 2.21; 95% CI 2.00-2.45) compared to unexposed controls. There was a dose-response relationship between severity of famine exposure and adult T2DM risk comparing individuals born in regions with severe, very severe, and extreme famine to births in the no-famine region.</p> <p> </p> <p><strong>Description of the data and analytical code</strong></p> <p>In exploratory analyses we first examined whether the odds for T2DM were elevated for any month of birth in the period January 1930 to December 1938 in any of the four regions of varying famine intensity. This was achieved by comparing, within each region, the T2DM odds for births in any month and year of birth relative to the T2DM odds for births in the same month combining all other years of birth. The analysis served to identify potential relations of famine with specific months and years of birth, controlling for month of birth effects. We observed increased T2DM odds ratios for births between January and June 1934 in famine-exposed oblasts, with smaller increases for births in 1935 and 1936 in these months. Our findings suggested that in multivariate modelling statistical control for month of birth effects could be accomplished by adjusting for the January-June period. Our findings are presented in the data file '01 Odds Ratio for T2DM Over Time' and show the odds ratios (ORs) for Type 2 Diabetes Mellitus (T2DM) comparing the region-specific T2DM odds for each birth year and month relative to births in the same months but combining all other years of birth. The R syntax file '01 Odds of T2DM Over Time Figure' provides the code necessary to reproduce the figure.</p> <p> </p> <p>For confirmatory analyses we employed a Difference-in-Differences approach to quantify associations between prenatal exposure to famine and T2DM, taking into account year of birth, half-year of birth (Jan-Jun vs Jul-Dec), region, and their interactions. This analysis was conducted initially for each gender separately and then for both genders combined, adjusting for We carried out sensitivity analyses to assess potential changes in T2DM odds arising from the use of pre-famine births vs post-famine births as controls. Our findings are presented in the data file '02 Ukraine Famine 1932-33 Main Data'. Information on the number of T2DM cases by gender, region of residence, and year and month of birth 1930-1938 in Ukraine was collected by the national Ukraine Diabetes Register (Komisarenko Institute of Endocrinology and Metabolism, Kyiv) between 2000-2008. The number of births in the same subgroups, representing the populations at risk for T2DM, was estimated by demographic population reconstruction methods as reported in the publication. We classified the birth counts by year of birth, the semi-annual birth period (January-June vs. July-December), region of birth, and gender. The SPSS syntax file titled '02 Ukraine Famine 1932-33 Main Analysis' provides the code to replicate our main findings as presented in the publication.</p> <p> </p> <p>In a separate analysis we visualized by a meta-regression approach the relation between famine intensity at the oblast level in 1933 and the odds for adult T2DM. The data required for the replication of our findings are included in the file '03 Odds Ratio for T2DM and Famine Intensity at Oblast Level'. The R syntax file titled '03 Ukraine Famine 1932-33 Meta-regression' provides details on conducting the meta-regression using the R package ‘metafor’.</p> <p> </p> <p><strong>Funding</strong></p> <p>Ukraine State complex program Diabetes Mellitus, project number 0106U000844 (M.K.). Holodomor Research and Education Consortium in Canada (L.H.L., O.W.). NIDI-NIAS Fellowship of the Royal Netherlands Academy of Sciences (L.H.L.). National Institute of Aging R01 AG028593 (L.H.L.). National Institute of Aging R01 AG06687 (L.H.L.).</p> <p> </p> <p><strong>Sharing/Access information</strong></p> <p>Data sharing and use are unrestricted with acknowledgement of the original publication and listing of the funding sources as per the above. Researchers are encouraged to contact the Principal Investigators (PIs) for consultations on data structure and use as needed (L.H. Lumey, <a href="mailto:lumey@columbia.edu">lumey@columbia.edu</a>; Oleh Wolowyna, <a href="mailto:olehw@aol.com">olehw@aol.com</a>).</p>
ScienceDex guides
Understand access before you commit
These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.